Reaktionsgleichung
[CH2:1]([NH:8][C@H:9](C)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:17]([Li])CCC.[CH3:22][O:23][C:24]1[N:29]=[CH:28][C:27]([CH:30]=[CH:31][C:32]([O:34][CH2:35][CH3:36])=[O:33])=[CH:26][CH:25]=1.[NH4+].[Cl-]>C1COCC1.CCCCCC.CCOC(C)=O>[CH2:35]([O:34][C:32](=[O:33])[C@H:31]([CH3:17])[C@@H:30]([C:27]1[CH:28]=[N:29][C:24]([O:23][CH3:22])=[CH:25][CH:26]=1)[N:8]([CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[CH2:9][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)[CH3:36]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a solution of N-benzyl-(R)-α-methylbenzylamine (97.5 g, 462 mmol) in THF (750 mL) at 0° C. was added n-butyllithium (2.5M in hexanes; 178.5 mL, 446 mmol). The dark violet solution was stirred at 0° C. for 20 minutes, cooled to −78° C., and the ester 16-3 (63.7 g, 308 mmol) in THF (250 mL) was added over 60 minutes. The resulting solution was stirred at −78° C. for 1 hr, then cannulated into saturated NH4Cl and extracted with EtOAc, washed with water then brine, dried and concentrated in vacuo to give an oil. Column chromatography (silica gel; hexane/EtOAc 9:1 then 4:1) gave 16-4 as an oil contaminated with N-benzyl-(R)-α-methylbenzylamine. This oil was taken up in 5% AcOH in water and extracted with diethyl ether (4×). The organic layers were dried over MgSO4 and the solvent removed to give the title compound 16-4.
Aufarbeitung
- temperaturecooled to −78° C.
- stirringThe resulting solution was stirred at −78° C. for 1 hr
- extractionextracted with EtOAc
- washwashed with water
- dry with materialbrine, dried
- concentrationconcentrated in vacuo
- customto give an oil
Quellen und Nachweise
- ORD-Eintrag
- ord-173e22320af243cfbb95bbdae789bfcb
- Quelldatensatz
- uspto-grants-2001_10
- Patentnummer
- US06297249B1
Verknüpfte Notizen
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